Jessica M. Maia, Ph.D.
Affiliations: | 2007 | North Carolina State University, Raleigh, NC |
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"Jessica Maia"Parents
Sign in to add mentor| Zhao-Bang Zeng | grad student | 2007 | NCSU | |
| (Joint analysis of multiple gene expression traits to map expression quantitative trait loci.) | ||||
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Publications
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| Long N, Dickson SP, Maia JM, et al. (2013) Leveraging prior information to detect causal variants via multi-variant regression. Plos Computational Biology. 9: e1003093 |
| Zhu M, Need AC, Han Y, et al. (2012) Using ERDS to infer copy-number variants in high-coverage genomes. American Journal of Human Genetics. 91: 408-21 |
| Zhu Q, Ge D, Heinzen EL, et al. (2012) Prioritizing genetic variants for causality on the basis of preferential linkage disequilibrium. American Journal of Human Genetics. 91: 422-34 |
| Need AC, McEvoy JP, Gennarelli M, et al. (2012) Exome sequencing followed by large-scale genotyping suggests a limited role for moderately rare risk factors of strong effect in schizophrenia. American Journal of Human Genetics. 91: 303-12 |
| Heinzen EL, Depondt C, Cavalleri GL, et al. (2012) Exome sequencing followed by large-scale genotyping fails to identify single rare variants of large effect in idiopathic generalized epilepsy. American Journal of Human Genetics. 91: 293-302 |
| Ge D, Ruzzo EK, Shianna KV, et al. (2011) SVA: software for annotating and visualizing sequenced human genomes. Bioinformatics (Oxford, England). 27: 1998-2000 |
| Zhu Q, Ge D, Maia JM, et al. (2011) A genome-wide comparison of the functional properties of rare and common genetic variants in humans. American Journal of Human Genetics. 88: 458-68 |
| Pelak K, Shianna KV, Ge D, et al. (2010) The characterization of twenty sequenced human genomes. Plos Genetics. 6: e1001111 |
| Cirulli ET, Singh A, Shianna KV, et al. (2010) Screening the human exome: a comparison of whole genome and whole transcriptome sequencing. Genome Biology. 11: R57 |
| Sobreira NL, Cirulli ET, Avramopoulos D, et al. (2010) Whole-genome sequencing of a single proband together with linkage analysis identifies a Mendelian disease gene. Plos Genetics. 6: e1000991 |